Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.238276865T>A | CA1338048964 | PER2 | c.293+266A>T (n.293+266A>T) | dbSNP |
2 | g.238276865T>C | CA11175891 | PER2 | c.293+266A>G (n.293+266A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.238276865T= | CA1338048963 | PER2 | c.293+266A= (n.293+266A=) | dbSNP |